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United States Patent |
6,155,977
|
Nowakowski
|
December 5, 2000
|
Method and apparatus for placement of a catheter
Abstract
The present invention provides a catheter which has an integral inflatable
and deflatable balloon. The catheter includes an elongated, flexible tube
and at least two spaced-apart openings therein. The operative element of
the catheter is in communication with the first opening of the tube. The
second opening in the catheter is in communication with the balloon.
Preferably, the balloon is made of latex and extends around the diameter
of the tube. Interfaces for both an inflation device for the balloon and a
control device for the operative element are connected to the trailing end
of the tube. The inflation device selectively inflates and deflates the
balloon. The control device controls the operative element of the
catheter. The catheter is placed by inserting the catheter with the
balloon in a deflated position into the specified body channel. The body
channel must have a restriction smaller than the size of the inflated
balloon. The catheter is introduced into the body such that the deflated
balloon passes through the restriction. At this point, the balloon is
inflated. The catheter is then withdrawn until the balloon is in contact
with the restriction. The balloon is then deflated and the catheter is in
position. To ensure proper placement of the operative element of the
catheter, the first opening must be an appropriate distance from the
balloon.
Inventors:
|
Nowakowski; Bogdan (2544 N. 65th Ave., Omaha, NE 68104)
|
Appl. No.:
|
311177 |
Filed:
|
May 13, 1999 |
Current U.S. Class: |
600/309; 604/192 |
Intern'l Class: |
A61B 005/00 |
Field of Search: |
604/192
600/309,342,343,361,350
|
References Cited
U.S. Patent Documents
5046497 | Sep., 1991 | Millar | 128/637.
|
5704353 | Jan., 1998 | Kalb et al. | 128/634.
|
5788631 | Aug., 1998 | Fiddian-Green | 600/309.
|
5928155 | Sep., 1999 | Eggers et al. | 600/526.
|
Other References
Digitrapper Mk III User's Manual Apr. 6, 1994 pp. 8-11 By Synectics Medical
AB.
|
Primary Examiner: Kennedy; Sharon
Assistant Examiner: Lam; Ann Y.
Attorney, Agent or Firm: Zarley, McKee, Thomte, Voorhees & Sease, Thomte; Dennis L.
Claims
I claim:
1. A flexible catheter for placement in a body channel having a region to
be monitored and a restriction of a given size therein, the restriction
and the region being separated by a distance, comprising:
an elongated flexible tube having leading and trailing ends and at least
first and second spaced-apart openings formed therein at a specified
distance from each other;
sensing means disposed in said tube in communication with said first
opening for collecting data;
conduit means positioned in said tube connected to said sensing means for
the communication of data collected by sensing means;
a selectively inflatable and deflatable balloon affixed to said tube
proximal said leading end and in communication with said second opening;
said balloon being inflatable to a size larger than that of the
restriction and being located a distance from said first opening equal to
the distance between the restriction and the region of the body channel to
be monitored; and
said trailing end of said tube adapted to be connected to a means for
inflating and deflating said balloon.
2. The flexible catheter of claim 1 wherein said tube includes additional
spaced-apart openings formed therein, which are positioned at specified
distances from each of said other openings, further comprising additional
sensing means, each additional sensing means being in communication with
and corresponding to an additional opening.
3. The flexible catheter of claim 2 wherein each of said additional sensing
means is connected to a discrete conduit means, each of said discrete
conduit means being housed within said tube.
4. The flexible catheter of claim 3 wherein said tube has an interior
surface and said balloon has an interior surface; said interior surface of
said tube and said interior surface of said balloon defining an airtight
chamber.
5. The flexible catheter of claim 3 wherein each of said sensing means
comprises a pH meter.
6. The flexible catheter of claim 1 wherein said sensing means comprises a
pH meter.
7. A method of placing a catheter in a body channel having a restriction of
a given size therein, comprising the steps of:
providing a catheter tube having spaced-apart first and second openings
therein;
positioning a sensing means within said catheter tube so that said sensing
means is in communication with said first opening;
positioning an inflatable and deflatable balloon on said catheter tube
which is in communication with said second opening and which is spaced
from said first opening a specified distance;
inserting said catheter into the body channel so that said balloon, in its
deflated condition, passes through the restriction;
inflating said balloon to a size larger than the size of the restriction;
withdrawing said catheter from the body channel until said balloon contacts
the restriction so that said sensing means is located at a specified
distance from the restriction; and
deflating said balloon.
8. A flexible catheter for placement in a body channel having a region in
which fluids are to be transferred and a restriction of a given size
therein, the restriction and the region being separated by a distance,
comprising:
an elongated flexible catheter tube having leading and trailing ends and at
least first and second spaced-apart openings at a specified distance from
each other;
a conduit means comprising an elongated, hollow interior tube positioned in
said catheter tube and having first and second ends, said interior tube
first end in communication with said first opening, said interior tube
second end positioned proximal said trailing end of said catheter tube for
transfer of fluids through said interior tube between the trailing end of
the catheter tube and the first opening therein;
a selectively inflatable and deflatable balloon affixed to said catheter
tube proximal said leading end and in communication with said second
opening; said balloon being inflatable to a size larger than that of the
restriction and being located a distance from said first opening equal to
the distance between the restriction and the region of the body channel
region in which fluids are to be transferred; and
said trailing end of said catheter adapted to be connected to means for
inflating and deflating said balloon.
9. The flexible catheter of claim 8 wherein said catheter tube includes
additional spaced-apart openings, formed therein which are positioned at
specified distances from each of said other openings, further comprising
additional elongated, hollow interior tubes, each additional interior tube
having a first end in communication with and corresponding to an
additional opening.
10. The flexible catheter of claim 9 wherein catheter tube has an interior
surface and said balloon has an interior surface; said interior surface of
said catheter tube, said interior surface of said balloon and said second
opening defining an air tight chamber.
11. A method of placing a catheter in a body channel having a restriction
of a given size therein and comprising the steps of:
providing a catheter tube having spaced-apart first therein;
positioning an elongated, hollow interior tube within said catheter tube,
said interior tube having a first end positioned in communication with
said first opening;
positioning an inflatable and deflatable balloon on said catheter tube
which is in communication with said second opening and which is spaced
from said first opening;
inserting said catheter into the body channel so that said balloon, in its
deflated condition, passes through the restriction;
inflating said balloon to a size larger than the size of the restriction;
withdrawing said catheter from the body channel until said balloon contacts
the restriction so that said first opening is located at a specified
distance from the restriction; and
deflating said balloon.
Description
BACKGROUND OF THE INVENTION
1. Technical Field
This invention relates generally to the placement of a catheter in a human
body and, more precisely, to the placement of a catheter within a channel
in the human body with the channel having a restriction therein.
2. Description of the Prior Art
Catheters have been used by health care professionals for some time. They
are generally used in the cardiopulmonary and gastrointestinal systems of
the body due to the fact that these systems include channels into which
the catheters are placed.
The catheters are used to introduce, measure, or extract fluids from the
body. Particularly with regard to measuring the properties of the fluid of
the body, proper placement of the catheter is of the utmost importance.
Proper placement of a catheter has been achieved by various means in the
past Certain catheters have been equipped with miniature video camera
capability. This allows the health care worker placing the catheter to see
the position of the catheter with respect to the body. While accurate,
this method has proven to be too expensive for many procedures.
Catheters have also been equipped with means for sensing ambient pressure
for the purpose of proper placement. For example, Synectics Medical AB has
developed a catheter, including a pressure sensing means, which is
designed to be placed in the upper gastrointestinal tract of a body. The
catheter is inserted into the nose of the patient and threaded into the
stomach of the patient. The catheter is then extracted slowly. The stomach
has comparatively lower ambient pressure than that of the lower esophagus.
The pressure sensing means is connected to an external meter which shows
the rise in ambient pressure. As the catheter is extracted, the pressure
sensing means enters the esophagus and the pressure on the pressure
sensing means rises. The catheter is then retained in this position.
The difference between the ambient pressure in the stomach and the ambient
pressure in the esophagus may be very small, inhibiting accurate placement
of the catheter. Also, the catheter must be extracted slowly. If the
catheter is extracted too quickly, the catheter may be misplaced and may
provide faulty data. Alternatively, the procedure may need to be repeated,
causing discomfort to the patient. For these reasons, extensive training
is required to place the existing catheters and, even with training,
proper placement is difficult.
It is a primary objective of the present invention to provide a catheter
which facilitates the proper placement thereof.
An additional objective is to provide a catheter that is inexpensive to
build and inexpensive to use based, in part, on minimal training required
to use it.
Another objective is to provide a catheter with an inflatable and
deflatable balloon as a part thereof.
Another object of the invention is to teach a method of placing such a
catheter precisely within a human body.
These and other objects will be apparent to those skilled in the art.
SUMMARY OF THE INVENTION
The catheter includes an elongated, flexible catheter tube having at least
two spaced-apart openings therein, and an integral inflatable and
deflatable balloon. The operative element of the catheter is in
communication with the first opening of the tube. The operative element of
the catheter may be a hollow tube positioned within the catheter tube for
the introduction or withdrawal of fluids from the body through the first
opening of the tube. The operative element may also be a meter or some
other instrument by which body fluids are sampled. The upper end of the
tube has an interface in communication with the operative element of the
catheter, to which the means for operating the catheter is operatively
connected. The second opening in the catheter is in communication with the
inflatable and deflatable balloon. Preferably, the balloon is made of
latex and extends around the diameter of the tube. The upper end of the
tube includes means for inflating the balloon or a connection to such
means. Such means may be a pump, vacuum, or remote meter for analyzing the
properties of body fluids.
The catheter is placed by inserting the catheter with the balloon deflated
into the specified body channel having a restriction smaller than the size
of the inflated balloon. The inflatable and deflatable balloon is
positioned on the tube with the interior thereof being in communication
with the second opening in the tube. The catheter is introduced into the
body such that the deflated balloon passes through the restriction, at
which time the balloon is inflated. The catheter is then withdrawn until
the balloon contacts or engages the restriction. The balloon is then
deflated and the catheter is in position. To ensure proper placement of
the operative element of the catheter, the first opening must be an
appropriate distance from the balloon.
BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a view of the catheter in place in the gastrointestinal system of
a human body.
FIG. 2 is a perspective view of the catheter.
FIG. 3 is an exploded view of the catheter enlarged to show detail.
DESCRIPTION OF THE PREFERRED EMBODIMENT
Referring now to the drawings, the catheter of the present invention is
designated generally by 10 and includes an elongated flexible tube 12.
Tube 12 must be narrow enough to fit within the body channel for which it
is designed. Tube 12 must also be long enough both to reach the area in
which the catheter is designed to operate and to allow the trailing end 14
to extend from the body.
Tube 12 is provided with at least a first opening 16 and a second opening
18. An operative element, such as a sensing means 20, is positioned within
and connected to the tube 12 such that an airtight seal is formed between
the sensing means 20 and the tube 12 around the first opening 16. This
structure exposes the sensing means 20 to the environment into which it is
introduced and prevents the introduction of body fluids into the tube 12.
The operative element may alternatively consist of a hollow tube for the
withdrawal or introduction of fluids from the body. The exterior wall of
the hollow tube must form an airtight seal with the wall of the tube 12
around the first opening 16 to allow fluids into the hollow tube, but not
into the tube 12.
An inflatable and deflatable resilient balloon 22 is attached to the
exterior of the tube 12, as seen in the drawings. Balloon 22 is,
preferably, designed to circumscribe tube 12 about the second opening 18.
Balloon 22 is connected to the tube 12 by a first annular seal 24 located
between the second opening 18 and the leading end 26 of the tube 12.
Balloon 22 is also connected to the tube 12 by a second annular seal 28
between the opening 18 and the trailing end 14 of the tube 12. Opening 16
must not be located between the first annular seal 24 and the second
annular seal 28, because balloon 22 will prevent the exposure of sensing
means 20 to the environment in which the catheter is placed.
The trailing end 14 of the tube 12 is connected to a conventional means for
operating catheter 10. As shown in FIG. 2, the trailing end 14 of tube 12
is connected to the means for operating catheter 10 by a T-shaped tubular
junction 32. Other means are available to connect tube 12 to the means for
operating catheter 10. The means for operating catheter 10 is comprised of
an interface 34 for a control device to operate the sensing means 20 and
an interface 36 for a conventional inflation device for inflating and
deflating balloon 22. The interface 34 is in operative communication with
the sensing means 20 by means of a conduit, such as relay 38. Where
different operative elements are used, the conduit may be comprised of
wires, tubes, or other media appropriate for the use of the control
device.
Catheter 10 is used in the manner more fully described below. Leading end
26 of the catheter 10 is inserted into the appropriate body channel with
the balloon 22 deflated. For proper placement, the body channel must have
at least one restriction which is narrower than the balloon 22 after the
balloon 22 has been inflated. Leading end 26 of the tube 12 is threaded
through the body channel until second annular seal 28 passes through the
channel restriction. An inflation device, not shown, is connected to the
interface 36 as previously described and may consist of a pump, a syringe,
or any other means of introduction of fluid. Interface 36 may be connected
to the second opening 18 by means of a discrete tube, or, preferably, it
may be connected directly to the tube 12 such that tube 12 and balloon 22
form a single airtight chamber.
The inflation device is activated to inflate balloon 22. While balloon 22
is still inflated, catheter 10 is withdrawn from the body until balloon 22
comes into contact with the restriction. First opening 16 must be located
on the tube 12 at a specific distance from the balloon 22 for the intended
purpose of the catheter 10. If, for instance, the user desires the sensing
means 20 to be placed within the body 5 cm past the restriction in the
body channel, opening 16 must be located between the balloon 22 and the
leading end 26 of the tube 12 and 5 cm from the second annular seal 28.
Similarly, if the operative element is designed to be placed in the body
at a position between the orifice into which the catheter is placed and
the restriction within the body channel, first opening 16 must be located
between the balloon 22 and the trailing end 14. The distance between the
balloon 22 and the first opening 16 will depend on the purpose for which
the catheter 10 is used, the size of the body in which the catheter 10 is
used, and other criteria.
More than one sensing means 20 may be used in conjunction with the catheter
10. Each or any of the sensing means 20 may be used to introduce, remove,
or measure fluids in the body. In the embodiment shown in FIGS. 1 and 2,
pH meters are accurately placed within the body by catheter 10. An opening
40 is located between the balloon 22 and the leading end 26 approximately
7 cm from the second annular seal 28. A first pH meter 42 is associated
with the opening 40 and measures the pH of fluids in the stomach. An
opening 44 is located between the balloon 22 and the trailing end 14
approximately 5 cm from second annular seal 28. A second pH meter 46 is
associated with the opening 44 and measures the pH of fluids in the lower
esophagus. An opening 48 is located between the balloon 22 and the
trailing end 14 approximately 20 cm from the second annular seal 28. A
third pH meter 50 is associated with the opening 48 and measures the pH of
the fluids in the upper esophagus. Each pH meter is connected by a conduit
38; in this instance, a wire, to the control device interface 34, which is
connected to a monitor or other device. Thus it can be seen that the
invention accomplishes at least all of its stated objectives.
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